70 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EKOS PE Endovascular Device with Control System 4.0 (CS4.0)
FDA 510(k)
FDA Class 2
·Cardiovascular
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964074974·Endo Carry-On Procedure Kit
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964077364·The ENDO CARRY-ON Procedure Kit contains all of...
Apelo® / Apelo® MIS
FDA UDI
ATLAS SPINE, INC.·M68120064800000·Collar Sleeve
SPIRO PRO
FDA 510(k)
FDA Class 2
·Anesthesiology
GRIDLOCK 195 ADHESIVE
FDA 510(k)
FDA Class 2
·Dental
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007
SYNCHROMED
FDA Adverse Event
Death
·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 16, 2024
UNK
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017
UNK
FDA Adverse Event
Death
·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017
UNK
FDA Adverse Event
Malfunction
·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·August 21, 2023